Exenatide-loaded inside-porous poly(lactic-co-glycolic acid) microspheres as a long-acting drug delivery system with improved release characteristics. (1st January 2020)

• Record Type: Journal Article
• Authors: Zhai, Junqiu; Ou, Zhanlun; Zhong, Liuting; Wang, Yu-e; Cao, Li-Ping; Guan, Shixia
• Is Part Of: Drug delivery. Volume 27:Number 1(2020)
• Page Start: 1667
• Page End: 1675
• Publication Date: 2020-01-01
• Subjects: Exenatide -- inside-porous microspheres -- long-acting -- release behavior -- type 2 diabetes; Drug delivery systems -- Periodicals; Drug targeting -- Periodicals; 615.05
• DOI: 10.1080/10717544.2020.1850919
• Languages: English
• ISSNs: 1071-7544

Abstract

Abstract: The glucagon-like peptide-1 receptor agonist exenatide (EXT) is an effective treatment for type 2 diabetes. However, this peptide has a short biological half-life and the delayed release characteristic of current formulations limit its clinical application. Herein, we prepared EXT-loaded inside-porous poly(d, l-lactic-co-glycolic acid (PLGA) microspheres with outside layers (EXT-PMS) using a W1 /O/W2 emulsion method with a microfluidic technique and its fabrication and formulation conditions were systematically investigated. In vitro dissolution experiments showed that the PLGA concentration, proportion of drug and oil phase, and the number and size of pores strongly affected the release behaviors of EXT-PMS. In vitro, the optimized EXT-PMS with large internal pores exhibited rapid and stable release without a lag phase. In a rat model, subcutaneous administration of the product yielded plasma concentrations of EXT that was sustained for 30 days with low burst and no delayed-release effect. The preparation of inside-porous microspheres is lighting up the development of long-acting drug delivery systems for other drugs with favorable release characteristics.